| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:46941406-46941570 | Common:2; Rare:46; Clinvar (benign):1 | ||||
| chr2:46941707-46941869 | Common:3; Rare:54; Clinvar (benign):1 | ||||
| chr2:46942220-46942438 | Common:3; Rare:48 | ||||
| chr2:46978173-46978226 | Rare:5 | ||||
| chr2:47175541-47176055 | Common:6; Rare:185 | ||||
| chr2:47176362-47176591 | Rare:149; Clinvar (benign):5 | ||||
| chr2:47176754-47177046 | Common:4; Rare:114 | ||||
| chr2:47402806-47403227 | Common:1; Rare:191; Clinvar:58; Clinvar (benign):34; Clinvar (pathogenic):1 | ||||
| chr2:47782769-47783243 | Common:4; Rare:201; Clinvar:8; Clinvar (benign):22; Clinvar (pathogenic):1 | ||||
| chr2:47783750-47783955 | Common:6; Rare:42; Clinvar (benign):2 | ||||
| chr2:47905325-47905444 | Common:2; Rare:49 | ||||
| chr2:48314104-48314267 | Rare:42 | ||||
| chr2:48314345-48314864 | Rare:189 | ||||
| chr2:48314875-48314963 | Common:1; Rare:41 | ||||
| chr2:48440419-48440921 | Common:10; Rare:189 |